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Copy pathfilter.py
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49 lines (40 loc) · 1.46 KB
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import sys
def read_fasta_sequences(fasta_file):
"""
从基因组序列文件中读取序列名列表
"""
genome_sequence_names = []
with open(fasta_file, 'r') as fasta:
for line in fasta:
if line.startswith('>'):
genome_sequence_names.append(line.strip()[1:])
return genome_sequence_names
def filter_gff_by_fasta(gff_file, genome_sequence_names):
"""
根据基因组序列名列表过滤注释文件,并输出到新文件中
"""
output_file = "filtered_" + gff_file
with open(gff_file, 'r') as gff, open(output_file, 'w') as filtered:
for line in gff:
if line.startswith('#'):
filtered.write(line)
continue
columns = line.strip().split('\t')
if len(columns) < 1:
continue
chromosome_name = columns[0]
if chromosome_name in genome_sequence_names:
filtered.write(line)
print(f"Filtered GFF file written to {output_file}")
if __name__ == "__main__":
if len(sys.argv) != 3:
print("Usage: python test.py <fasta_file> <gff_file>")
sys.exit(1)
fasta_file = sys.argv[1]
gff_file = sys.argv[2]
try:
genome_sequence_names = read_fasta_sequences(fasta_file)
filter_gff_by_fasta(gff_file, genome_sequence_names)
except FileNotFoundError as e:
print(f"Error: {e}")
sys.exit(1)